Label: NU SKIN SUNRIGHT LIP BALM BROAD SPECTRUM SPF 15- octinoxate, avobenzone, and octocrylene stick
- NDC Code(s): 62839-6201-1
- Packager: NSE Products, Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 14, 2022
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
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Use
- Helps prevent sunburn. Higher SPF gives more sunburn protection.
- If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
- Warnings
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Directions
- Sunprotection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m.–2 p.m. Wear long-sleeved shirts, pants, hats, and sunglasses.
- Apply liberally 15 minutes before sun exposure.
- Reapply at least every two hours.
- Use a water resistant sunscreen if swimming or sweating.
- Children under 6 months: Ask a doctor.
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Inactive Ingredients
Ricinus Communis (Castor) Seed Oil, Helianthus Annuus (Sunflower) Seed Oil, Beeswax, Euphorbia Cerifera (Candelilla) Wax, Ozokerite, Polyethylene, Caprylic/Capric Triglyceride, Octyldodecyl Neopentanoate, Flavor (Aroma), Glycine Soja (Soybean) Oil, Ethyl Vanillin, Chlorella Vulgaris Extract, Tocopherol, Tocopheryl Acetate, Zea Mays (Corn) Starch, Silica, Water (Aqua), Ethylhexylglycerin, Phenoxyethanol.
- Other Information
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- PRINCIPAL DISPLAY PANEL - 15 ml Tube Pouch Label
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INGREDIENTS AND APPEARANCE
NU SKIN SUNRIGHT LIP BALM BROAD SPECTRUM SPF 15
octinoxate, avobenzone, and octocrylene stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-6201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 75 mg in 1 mL Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 30 mg in 1 mL Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 27.9 mg in 1 mL Inactive Ingredients Ingredient Name Strength CASTOR OIL (UNII: D5340Y2I9G) SUNFLOWER OIL (UNII: 3W1JG795YI) CANDELILLA WAX (UNII: WL0328HX19) YELLOW WAX (UNII: 2ZA36H0S2V) CERESIN (UNII: Q1LS2UJO3A) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) SOYBEAN OIL (UNII: 241ATL177A) ETHYL VANILLIN (UNII: YC9ST449YJ) PHENOXYETHANOL (UNII: HIE492ZZ3T) STARCH, CORN (UNII: O8232NY3SJ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TOCOPHEROL (UNII: R0ZB2556P8) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WATER (UNII: 059QF0KO0R) CHLORELLA VULGARIS (UNII: RYQ4R60M02) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-6201-1 1 in 1 POUCH 07/01/2014 1 15 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part352 07/01/2014 Labeler - NSE Products, Inc. (803486393)
